scholarly journals Case report: Acute Localized Exanthematous Pustulosis Following mRNA-1273 SARS-CoV-2 Vaccination

2021 ◽  
Vol 8 (5) ◽  
pp. 01-03
Author(s):  
Peter A. Young ◽  
Jessica B. Chan ◽  
Michael W. Su
Keyword(s):  
Case Report ◽  
T Cell ◽  
Young Adult ◽  
Inflammatory Response ◽  
Adult Female ◽  
Messenger Rna ◽  
Clinical Appearance ◽  
Acute Generalized Exanthematous Pustulosis ◽  
The Face ◽  
Exanthematous Pustulosis

Acute localized exanthematous pustulosis (ALEP) is a rare subtype of acute generalized exanthematous pustulosis (AGEP) with identical histologic findings. It results from a T-cell related neutrophilic inflammatory response and is characterized by monomorphic sterile pustules confined to the face, neck, or chest. Two cases of similar facial pustular eruptions in association with the messenger RNA–1273 SARS-CoV-2 vaccine have been reported, both in males of lighter skin over 50 years old. To highlight this rare reaction and its clinical appearance in patients of pigment-rich skin, we report the case of a young adult female with ALEP following injection of the RNA–1273 SARS-CoV-2 vaccine.

scholarly journals Primary cutaneous CD4+ small/medium T-cell lymphoma: a case report

2021 ◽  
Vol 22 (4) ◽  
pp. 199-203
Author(s):  
Jeenam Kim ◽  
Minkyoung Jeong ◽  
Dongkeun Jun ◽  
Myungchul Lee ◽  
Donghyeok Shin ◽  
...  
Keyword(s):  
Case Report ◽  
T Cell ◽  
Lymphoproliferative Disorder ◽  
Cell Lymphoma ◽  
Surgical Excision ◽  
Lymphoid Cells ◽  
The Face ◽  
Single Mass ◽  
Histopathologic Findings

Primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder is a rare disease characterized by a single mass on the face or upper part of the trunk. It usually presents an asymptomatic and favorable progression, and its histopathologic findings include small and medium-sized lymphoid cells. The authors report a case of primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder on the forehead. A 51-year-old man presented with a protruding mass on his forehead that the patient had noted 1 month previously. Surgical excision and a permanent biopsy were performed under local anesthesia. Based on the biopsy results, the mass was diagnosed as a primary cutaneous CD4+ small/medium T-cell lymphoproliferative disorder. There was no evidence of recurrence at a 15-month follow-up visit.

scholarly journals Primary adrenal T-cell lymphoma in a young adult presented with pseudo-hypopyon: a case report and literature review

2017 ◽  
Vol 52 (3) ◽  
pp. 227 ◽  
Author(s):  
Karthik Bommannan ◽  
Man Updesh Singh Sachdeva ◽  
Aravind Sekar ◽  
Rajender Kumar ◽  
Pranab Dey
Keyword(s):  
Case Report ◽  
T Cell ◽  
Young Adult ◽  
Literature Review ◽  
Cell Lymphoma ◽  
T Cell Lymphoma

Acute generalized exanthematous pustulosis induced by iron carboxymaltose infusion: A case report

2020 ◽  
Vol 33 (3) ◽  
Author(s):  
Ecem Bostan ◽  
Huseyin Berk Yalcin ◽  
Neslihan Akdogan ◽  
Deniz Ates Ozdemir ◽  
Aysen Karaduman
Keyword(s):  
Case Report ◽  
Acute Generalized Exanthematous Pustulosis ◽  
Exanthematous Pustulosis

Acute Generalized Exanthematous Pustulosis Induced by Docetaxel and Recurrent With Letrozole: A Case Report

2018 ◽  
Vol 18 (5) ◽  
pp. e743-e746 ◽  
Author(s):  
Victor Sarradin ◽  
Florence Dalenc ◽  
Vincent Sibaud ◽  
Emilie Tournier ◽  
Henri Roché
Keyword(s):  
Case Report ◽  
Acute Generalized Exanthematous Pustulosis ◽  
Exanthematous Pustulosis
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